| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126861897, MYH7 (A1763T) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +11 more | |
| | LOC126861897, MHRT
+1 more (R1677H) | Single nucleotide variant (non-coding transcript variant +1 more) | MYH7-related condition +11 more | |
| | LOC126861897, MHRT
+1 more (R1662H) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified +3 more | GConflicting classifications of pathogenicity |
| | MHRT, LOC126861897
+1 more (R1608C) | Single nucleotide variant (non-coding transcript variant +1 more) | Cardiomyopathy +2 more | |
| | LOC126861897, MHRT
+1 more (A1603V) | Single nucleotide variant (non-coding transcript variant +1 more) | Primary dilated cardiomyopathy | |
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